This non-randomized, multicenter feasibility clinical study is designed to evaluate the safety and efficacy of the DASCOR Disc Arthoplasty Device in subjects with degenerative disc disease (DDD) of the lumbar spine from L2 to the sacrum and to provide data for use in hypothesis and endpoint determination for the DASCOR 3D Pivotal Study

For information about this study please contact:  Crystal Hill at (919) 281-1870 or email at chill@triangleortho.com .